Variant #0000880233 (NC_000009.11:g.154737C>A, NM_018491.3:c.634G>T (CBWD1))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.154737C>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CBWD1_000031
Frequency 1/7302
Freq. EA 1/4592
Freq. AA 0/2710
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:29:58 +02:00 (CEST)
Date last edited 2020-08-30 01:16:06 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CBWD1 NM_018491.3 ?/? c.634G>T r.(?) p.(Asp212Tyr)